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Filter SNVs Using Feature Selection

Chromosome chr1 chr2 chr3 chr4 chr5 chr6 chr7 chr8 chr9 chr10 chr11 chr12 chr13 chr14 chr15 chr16 chr17 chr18 chr19 chr20
Individual All CR1 CR2 CR3 TW1 JM1 JM2 CE1 CE2 CE3 CE4 CE5 TM1 TM2 AM1 SM1 SM2 PM1 PM2 LM1 BM1
Gene feature All CDS EXON 3'UTR INTRON 5'UTR Genotype All homozygote heterozygote Mutation All non-synonymous synonymous
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715422 SNVs 1 of 71543 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP011005515239 chr2: 34364 CE5 Intergenic C T
heterozygote
MACSNP011005515258 chr2: 35762 CE5 Intergenic A T
homozygote
MACSNP011005515268 chr2: 37287 CE5 Intergenic T G
heterozygote
MACSNP011005515270 chr2: 37608 CE5 Intergenic T C
heterozygote
MACSNP011005515279 chr2: 38356 CE5 Intergenic C A
heterozygote
MACSNP011005515288 chr2: 38958 CE5 Intergenic A T
heterozygote
MACSNP011005515291 chr2: 39585 CE5 Intergenic A G
heterozygote
MACSNP011005515292 chr2: 39593 CE5 Intergenic G C
heterozygote
MACSNP011005515307 chr2: 41067 CE5 Intergenic C T
homozygote
MACSNP011005515313 chr2: 41574 CE5 Intergenic T C
heterozygote

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